Comments (2)
Would like to know as well. I found the reformatted gtf contains bambu generated transcripts with sequin, but not sure if these are complete sequin transcripts.
from sg-nex-data.
Hi,
Sorry for getting back lately.
For the sequin reference, you may download the fasta and gtf file using the links below:
gtf file: http://sg-nex-data.s3.amazonaws.com/data/annotations/gtf_file/hg38_sequins_SIRV_ERCCs_longSIRVs_v5_reformatted.gtf
this is the complete gtf file that we used for our analysis, for your case, you can subset the gtf file to only sequin annotations, filtering by either sequin gene or transcript names
fasta file:
http://sg-nex-data.s3.amazonaws.com/data/annotations/genome_fasta/hg38_sequins_SIRV_ERCCs_longSIRVs.fa
similarly for the fasta file, you can also extract only the sequences for sequins by looking at chrIS only
For the sequin concentration, we have recently added the concentration file that we have used for the original manuscript: https://github.com/GoekeLab/sg-nex-data/blob/master/docs/RNAsequins_MixA.xlsx
Let me know you still have issues related to this.
Thank you
from sg-nex-data.
Related Issues (16)
- Fast5 files HOT 3
- Data Release? HOT 2
- sample_id SGNex_MCF7-EV_directRNA_replicate2_run1 is duplicate HOT 1
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- two fastq files were not correctly formated HOT 3
- Sequin spike-in reference HOT 4
- Identification of m6A with the SG-NEx samples HOT 1
- RNA004 data HOT 2
- No download for fastq HOT 2
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from sg-nex-data.